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FDA 510(k), K183198, FlowTriever Retrieval/Aspiration System
FDA 510(k), K183198, FlowTriever Retrieval/Aspiration System
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510(K) Number: K183198
Device Name: FlowTriever Retrieval/Aspiration System
Manufacturer: Inari Medical
Device Classification Name: peripheral mechanical thrombectomy with aspiration
Regulation Number: 870.5150
Classification Product Code: QEW
Date Received: 11/19/2018
Decision Date: 12/17/2018
Regulation Medical Specialty: Cardiovascular
Device Name: FlowTriever Retrieval/Aspiration System
Manufacturer: Inari Medical
Device Classification Name: peripheral mechanical thrombectomy with aspiration
Regulation Number: 870.5150
Classification Product Code: QEW
Date Received: 11/19/2018
Decision Date: 12/17/2018
Regulation Medical Specialty: Cardiovascular
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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